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This is VAERS ID 311332

History of Changes from the VAERS Wayback Machine

First Appeared on 12/8/2009

VAERS ID: 311332
VAERS Form:
Age:0.6
Gender:Female
Location:Foreign
Vaccinated:2007-10-01
Onset:2008-02-12
Submitted:2008-04-30
Entered:2008-04-30
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HEP: HEP B (NO BRAND NAME) / UNKNOWN MANUFACTURER - / 1 UN / IM
PPV: PNEUMO (NO BRAND NAME) / UNKNOWN MANUFACTURER - / 1 UN / IM
ROTH1: ROTAVIRUS (ROTARIX) / GLAXOSMITHKLINE BIOLOGICALS - / 1 - / PO

Administered by: Other      Purchased by: Other
Symptoms: Abdominal pain, Appendicectomy, Crying, Dehydration, Haematochezia, Inappropriate schedule of drug administration, Intussusception, Irritability, Surgery, Vomiting, Gastrointestinal hypermotility, Abdominal X-ray

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit (V2.0)? No
ER or Office Visit (V1.0)? No
ER or ED Visit (V2.0)? No
Hospitalized? Yes, days: 7     Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness: Unknown
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Abdominal X-ray 14Feb2008 Abnormal unit
CDC 'Split Type': B0517193A

Write-up: This case was reported by a physician and described the occurrence of intussusception in a 11-month-old female subject who was vaccinated with ROTARIX (GlaxoSmithKline). Previous and/or concurrent vaccination included combined diphtheria, tetanus, acellular pertussis, inactivated poliomyelitis and Haemophilus influenzae type b vaccine; manufacturer unspecified; intramuscular; given on 31 July 2007, 4 December 2007 and an unspecified date; hepatitis B vaccine recombinant; manufacturer unspecified; intramuscular; given on 31 July 2007, 1 October 2007 and 4 December 2007; influenza virus vaccine; manufacturer unspecified; intramuscular; given on 4 December 2007; live attenuated human rotavirus vaccine; GlaxoSmithKline; oral given on 31 July 2007; pneumococcal vaccine, unspecified; manufacturer unspecified; intramuscular; given on 31 July 2007 and 1 October 2007; tuberculosis vaccine; manufacturer unspecified; intradermal; given on 9 February 2008. On 1 October 2007, the subject received 2nd dose of ROTARIX (oral), lot number not provided. On 12 February 2008, 4 months after vaccination with ROTARIX, the subject experienced gastric vomiting followed by biliary vomiting with colic and abdominal pain. She had not flatulence nor fever. On 13 February 2008, the subject was hospitalised for 7 days. Physical examination showed abdominal pain with increased peristalsis, dehydration, irritability, crying at abdominal palpation, non-tender abdomen with respiratory pathology. On 14 February 2008, the subject experienced bloody stools as well as biliary vomiting. The rectal examination revealed an empty ampulla with blood. Abdomen X-ray showed fluid levels and dilated bowel loops with non-specific abnormalities. No intussusception was found. The surgery was performed and intussusception of ascending and descending colon was found and resolved by taxis without complication. A prophylactic appendectomy was performed. On 19 February 2008, the events were resolved and the subject was discharged from hospital in good clinical condit


Changed on 5/13/2013

VAERS ID: 311332 Before After
VAERS Form:
Age:0.6
Gender:Female
Location:Foreign
Vaccinated:2007-10-01
Onset:2008-02-12
Submitted:2008-04-30
Entered:2008-04-30
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HEP: HEP B (NO BRAND NAME) / UNKNOWN MANUFACTURER - / 1 UN / IM
PPV: PNEUMO (NO BRAND NAME) / UNKNOWN MANUFACTURER - / 1 UN / IM
ROTH1: ROTAVIRUS (ROTARIX) / GLAXOSMITHKLINE BIOLOGICALS - / 1 - / PO
RV1: ROTAVIRUS (ROTARIX) / GLAXOSMITHKLINE BIOLOGICALS - / 1 - / PO

Administered by: Other      Purchased by: Other
Symptoms: Abdominal pain, Appendicectomy, Crying, Dehydration, Haematochezia, Inappropriate schedule of drug administration, Intussusception, Irritability, Surgery, Vomiting, Gastrointestinal hypermotility, Abdominal X-ray

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit (V2.0)? No
ER or Office Visit (V1.0)? No
ER or ED Visit (V2.0)? No
Hospitalized? Yes, days: 7     Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness: Unknown
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Abdominal X-ray 14Feb2008 Abnormal unit
CDC 'Split Type': B0517193A

Write-up: This case was reported by a physician and described the occurrence of intussusception in a 11-month-old female subject who was vaccinated with ROTARIX (GlaxoSmithKline). Previous and/or concurrent vaccination included combined diphtheria, tetanus, acellular pertussis, inactivated poliomyelitis and Haemophilus influenzae type b vaccine; manufacturer unspecified; intramuscular; given on 31 July 2007, 4 December 2007 and an unspecified date; hepatitis B vaccine recombinant; manufacturer unspecified; intramuscular; given on 31 July 2007, 1 October 2007 and 4 December 2007; influenza virus vaccine; manufacturer unspecified; intramuscular; given on 4 December 2007; live attenuated human rotavirus vaccine; GlaxoSmithKline; oral given on 31 July 2007; pneumococcal vaccine, unspecified; manufacturer unspecified; intramuscular; given on 31 July 2007 and 1 October 2007; tuberculosis vaccine; manufacturer unspecified; intradermal; given on 9 February 2008. On 1 October 2007, the subject received 2nd dose of ROTARIX (oral), lot number not provided. On 12 February 2008, 4 months after vaccination with ROTARIX, the subject experienced gastric vomiting followed by biliary vomiting with colic and abdominal pain. She had not flatulence nor fever. On 13 February 2008, the subject was hospitalised for 7 days. Physical examination showed abdominal pain with increased peristalsis, dehydration, irritability, crying at abdominal palpation, non-tender abdomen with respiratory pathology. On 14 February 2008, the subject experienced bloody stools as well as biliary vomiting. The rectal examination revealed an empty ampulla with blood. Abdomen X-ray showed fluid levels and dilated bowel loops with non-specific abnormalities. No intussusception was found. The surgery was performed and intussusception of ascending and descending colon was found and resolved by taxis without complication. A prophylactic appendectomy was performed. On 19 February 2008, the events were resolved and the subject was discharged from hospital in good clinical condit


Changed on 4/14/2017

VAERS ID: 311332 Before After
VAERS Form:
Age:0.6
Gender:Female
Location:Foreign
Vaccinated:2007-10-01
Onset:2008-02-12
Submitted:2008-04-30
Entered:2008-04-30
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HEP: HEP B (NO BRAND NAME) / UNKNOWN MANUFACTURER - / 1 UN / IM
PPV: PNEUMO (NO BRAND NAME) / UNKNOWN MANUFACTURER - / 1 UN / IM
RV1: ROTAVIRUS (ROTARIX) / GLAXOSMITHKLINE BIOLOGICALS - / 1 - / PO

Administered by: Other      Purchased by: Other
Symptoms: Abdominal pain, Appendicectomy, Crying, Dehydration, Haematochezia, Inappropriate schedule of drug administration, Intussusception, Irritability, Surgery, Vomiting, Gastrointestinal hypermotility, Abdominal X-ray

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit (V2.0)? No
ER or Office Visit (V1.0)? No
ER or ED Visit (V2.0)? No
Hospitalized? Yes, days: 7     Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness: Unknown
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Abdominal X-ray 14Feb2008 Abnormal unit
CDC 'Split Type': B0517193A

Write-up: This case was reported by a physician and described the occurrence of intussusception in a 11-month-old female subject who was vaccinated with ROTARIX (GlaxoSmithKline). Previous and/or concurrent vaccination included combined diphtheria, tetanus, acellular pertussis, inactivated poliomyelitis and Haemophilus influenzae type b vaccine; manufacturer unspecified; intramuscular; given on 31 July 2007, 4 December 2007 and an unspecified date; hepatitis B vaccine recombinant; manufacturer unspecified; intramuscular; given on 31 July 2007, 1 October 2007 and 4 December 2007; influenza virus vaccine; manufacturer unspecified; intramuscular; given on 4 December 2007; live attenuated human rotavirus vaccine; GlaxoSmithKline; oral given on 31 July 2007; pneumococcal vaccine, unspecified; manufacturer unspecified; intramuscular; given on 31 July 2007 and 1 October 2007; tuberculosis vaccine; manufacturer unspecified; intradermal; given on 9 February 2008. On 1 October 2007, the subject received 2nd dose of ROTARIX (oral), lot number not provided. On 12 February 2008, 4 months after vaccination with ROTARIX, the subject experienced gastric vomiting followed by biliary vomiting with colic and abdominal pain. She had not flatulence nor fever. On 13 February 2008, the subject was hospitalised for 7 days. Physical examination showed abdominal pain with increased peristalsis, dehydration, irritability, crying at abdominal palpation, non-tender abdomen with respiratory pathology. On 14 February 2008, the subject experienced bloody stools as well as biliary vomiting. The rectal examination revealed an empty ampulla with blood. Abdomen X-ray showed fluid levels and dilated bowel loops with non-specific abnormalities. No intussusception was found. The surgery was performed and intussusception of ascending and descending colon was found and resolved by taxis without complication. A prophylactic appendectomy was performed. On 19 February 2008, the events were resolved and the subject was discharged from hospital in good clinical condit condition. The physician considered the events were unrelated to vaccination with ROTARIX.


Changed on 9/14/2017

VAERS ID: 311332 Before After
VAERS Form:(blank) 1
Age:0.6
Gender:Female
Location:Foreign
Vaccinated:2007-10-01
Onset:2008-02-12
Submitted:2008-04-30
Entered:2008-04-30
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HEP: HEP B (NO BRAND NAME) / UNKNOWN MANUFACTURER - / 1 2 UN / IM
PPV: PNEUMO (NO BRAND NAME) / UNKNOWN MANUFACTURER - / 1 2 UN / IM
RV1: ROTAVIRUS (ROTARIX) / GLAXOSMITHKLINE BIOLOGICALS - / 1 2 - MO / PO

Administered by: Other      Purchased by: Other
Symptoms: Abdominal pain, Appendicectomy, Crying, Dehydration, Haematochezia, Inappropriate schedule of drug administration, Intussusception, Irritability, Surgery, Vomiting, Gastrointestinal hypermotility, Abdominal X-ray

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit (V2.0)? No
ER or Office Visit (V1.0)? No
ER or ED Visit (V2.0)? No
Hospitalized? Yes, days: 7     Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness: Unknown
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Abdominal X-ray 14Feb2008 Abnormal unit
CDC 'Split Type': B0517193A

Write-up: This case was reported by a physician and described the occurrence of intussusception in a 11-month-old female subject who was vaccinated with ROTARIX (GlaxoSmithKline). Previous and/or concurrent vaccination included combined diphtheria, tetanus, acellular pertussis, inactivated poliomyelitis and Haemophilus influenzae type b vaccine; manufacturer unspecified; intramuscular; given on 31 July 2007, 4 December 2007 and an unspecified date; hepatitis B vaccine recombinant; manufacturer unspecified; intramuscular; given on 31 July 2007, 1 October 2007 and 4 December 2007; influenza virus vaccine; manufacturer unspecified; intramuscular; given on 4 December 2007; live attenuated human rotavirus vaccine; GlaxoSmithKline; oral given on 31 July 2007; pneumococcal vaccine, unspecified; manufacturer unspecified; intramuscular; given on 31 July 2007 and 1 October 2007; tuberculosis vaccine; manufacturer unspecified; intradermal; given on 9 February 2008. On 1 October 2007, the subject received 2nd dose of ROTARIX (oral), lot number not provided. On 12 February 2008, 4 months after vaccination with ROTARIX, the subject experienced gastric vomiting followed by biliary vomiting with colic and abdominal pain. She had not flatulence nor fever. On 13 February 2008, the subject was hospitalised for 7 days. Physical examination showed abdominal pain with increased peristalsis, dehydration, irritability, crying at abdominal palpation, non-tender abdomen with respiratory pathology. On 14 February 2008, the subject experienced bloody stools as well as biliary vomiting. The rectal examination revealed an empty ampulla with blood. Abdomen X-ray showed fluid levels and dilated bowel loops with non-specific abnormalities. No intussusception was found. The surgery was performed and intussusception of ascending and descending colon was found and resolved by taxis without complication. A prophylactic appendectomy was performed. On 19 February 2008, the events were resolved and the subject was discharged from hospital in good clinical condition. The physician considered the events were unrelated to vaccination with ROTARIX.


Changed on 2/14/2018

VAERS ID: 311332 Before After
VAERS Form:1
Age:0.6
Gender:Female
Location:Foreign
Vaccinated:2007-10-01
Onset:2008-02-12
Submitted:2008-04-30
Entered:2008-04-30
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HEP: HEP B (NO BRAND NAME) / UNKNOWN MANUFACTURER - / 2 UN / IM
PPV: PNEUMO (NO BRAND NAME) / UNKNOWN MANUFACTURER - / 2 UN / IM
RV1: ROTAVIRUS (ROTARIX) / GLAXOSMITHKLINE BIOLOGICALS - / 2 MO / PO

Administered by: Other      Purchased by: Other
Symptoms: Abdominal pain, Appendicectomy, Crying, Dehydration, Haematochezia, Inappropriate schedule of drug administration, Intussusception, Irritability, Surgery, Vomiting, Gastrointestinal hypermotility, Abdominal X-ray

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit (V2.0)? No
ER or Office Visit (V1.0)? No
ER or ED Visit (V2.0)? No
Hospitalized? Yes, days: 7     Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness: Unknown
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Abdominal X-ray 14Feb2008 Abnormal unit
CDC 'Split Type': B0517193A

Write-up: This case was reported by a physician and described the occurrence of intussusception in a 11-month-old female subject who was vaccinated with ROTARIX (GlaxoSmithKline). Previous and/or concurrent vaccination included combined diphtheria, tetanus, acellular pertussis, inactivated poliomyelitis and Haemophilus influenzae type b vaccine; manufacturer unspecified; intramuscular; given on 31 July 2007, 4 December 2007 and an unspecified date; hepatitis B vaccine recombinant; manufacturer unspecified; intramuscular; given on 31 July 2007, 1 October 2007 and 4 December 2007; influenza virus vaccine; manufacturer unspecified; intramuscular; given on 4 December 2007; live attenuated human rotavirus vaccine; GlaxoSmithKline; oral given on 31 July 2007; pneumococcal vaccine, unspecified; manufacturer unspecified; intramuscular; given on 31 July 2007 and 1 October 2007; tuberculosis vaccine; manufacturer unspecified; intradermal; given on 9 February 2008. On 1 October 2007, the subject received 2nd dose of ROTARIX (oral), lot number not provided. On 12 February 2008, 4 months after vaccination with ROTARIX, the subject experienced gastric vomiting followed by biliary vomiting with colic and abdominal pain. She had not flatulence nor fever. On 13 February 2008, the subject was hospitalised for 7 days. Physical examination showed abdominal pain with increased peristalsis, dehydration, irritability, crying at abdominal palpation, non-tender abdomen with respiratory pathology. On 14 February 2008, the subject experienced bloody stools as well as biliary vomiting. The rectal examination revealed an empty ampulla with blood. Abdomen X-ray showed fluid levels and dilated bowel loops with non-specific abnormalities. No intussusception was found. The surgery was performed and intussusception of ascending and descending colon was found and resolved by taxis without complication. A prophylactic appendectomy was performed. On 19 February 2008, the events were resolved and the subject was discharged from hospital in good clinical condition. The physician considered the events were unrelated to vaccination with ROTARIX.


Changed on 6/14/2018

VAERS ID: 311332 Before After
VAERS Form:1
Age:0.6
Gender:Female
Location:Foreign
Vaccinated:2007-10-01
Onset:2008-02-12
Submitted:2008-04-30
Entered:2008-04-30
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HEP: HEP B (NO BRAND NAME) / UNKNOWN MANUFACTURER - / 2 UN / IM
PPV: PNEUMO (NO BRAND NAME) / UNKNOWN MANUFACTURER - / 2 UN / IM
RV1: ROTAVIRUS (ROTARIX) / GLAXOSMITHKLINE BIOLOGICALS - / 2 MO / PO

Administered by: Other      Purchased by: Other
Symptoms: Abdominal pain, Appendicectomy, Crying, Dehydration, Haematochezia, Inappropriate schedule of drug administration, Intussusception, Irritability, Surgery, Vomiting, Gastrointestinal hypermotility, Abdominal X-ray

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit (V2.0)? No
ER or Office Visit (V1.0)? No
ER or ED Visit (V2.0)? No
Hospitalized? Yes, days: 7     Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness: Unknown
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Abdominal X-ray 14Feb2008 Abnormal unit
CDC 'Split Type': B0517193A

Write-up: This case was reported by a physician and described the occurrence of intussusception in a 11-month-old female subject who was vaccinated with ROTARIX (GlaxoSmithKline). Previous and/or concurrent vaccination included combined diphtheria, tetanus, acellular pertussis, inactivated poliomyelitis and Haemophilus influenzae type b vaccine; manufacturer unspecified; intramuscular; given on 31 July 2007, 4 December 2007 and an unspecified date; hepatitis B vaccine recombinant; manufacturer unspecified; intramuscular; given on 31 July 2007, 1 October 2007 and 4 December 2007; influenza virus vaccine; manufacturer unspecified; intramuscular; given on 4 December 2007; live attenuated human rotavirus vaccine; GlaxoSmithKline; oral given on 31 July 2007; pneumococcal vaccine, unspecified; manufacturer unspecified; intramuscular; given on 31 July 2007 and 1 October 2007; tuberculosis vaccine; manufacturer unspecified; intradermal; given on 9 February 2008. On 1 October 2007, the subject received 2nd dose of ROTARIX (oral), lot number not provided. On 12 February 2008, 4 months after vaccination with ROTARIX, the subject experienced gastric vomiting followed by biliary vomiting with colic and abdominal pain. She had not flatulence nor fever. On 13 February 2008, the subject was hospitalised for 7 days. Physical examination showed abdominal pain with increased peristalsis, dehydration, irritability, crying at abdominal palpation, non-tender abdomen with respiratory pathology. On 14 February 2008, the subject experienced bloody stools as well as biliary vomiting. The rectal examination revealed an empty ampulla with blood. Abdomen X-ray showed fluid levels and dilated bowel loops with non-specific abnormalities. No intussusception was found. The surgery was performed and intussusception of ascending and descending colon was found and resolved by taxis without complication. A prophylactic appendectomy was performed. On 19 February 2008, the events were resolved and the subject was discharged from hospital in good clinical condition. The physician considered the events were unrelated to vaccination with ROTARIX.


Changed on 8/14/2018

VAERS ID: 311332 Before After
VAERS Form:1
Age:0.6
Gender:Female
Location:Foreign
Vaccinated:2007-10-01
Onset:2008-02-12
Submitted:2008-04-30
Entered:2008-04-30
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HEP: HEP B (NO BRAND NAME) / UNKNOWN MANUFACTURER - / 2 UN / IM
PPV: PNEUMO (NO BRAND NAME) / UNKNOWN MANUFACTURER - / 2 UN / IM
RV1: ROTAVIRUS (ROTARIX) / GLAXOSMITHKLINE BIOLOGICALS - / 2 MO / PO

Administered by: Other      Purchased by: Other
Symptoms: Abdominal pain, Appendicectomy, Crying, Dehydration, Haematochezia, Inappropriate schedule of drug administration, Intussusception, Irritability, Surgery, Vomiting, Gastrointestinal hypermotility, Abdominal X-ray

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit (V2.0)? No
ER or Office Visit (V1.0)? No
ER or ED Visit (V2.0)? No
Hospitalized? Yes, days: 7     Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness: Unknown
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Abdominal X-ray 14Feb2008 Abnormal unit
CDC 'Split Type': B0517193A

Write-up: This case was reported by a physician and described the occurrence of intussusception in a 11-month-old female subject who was vaccinated with ROTARIX (GlaxoSmithKline). Previous and/or concurrent vaccination included combined diphtheria, tetanus, acellular pertussis, inactivated poliomyelitis and Haemophilus influenzae type b vaccine; manufacturer unspecified; intramuscular; given on 31 July 2007, 4 December 2007 and an unspecified date; hepatitis B vaccine recombinant; manufacturer unspecified; intramuscular; given on 31 July 2007, 1 October 2007 and 4 December 2007; influenza virus vaccine; manufacturer unspecified; intramuscular; given on 4 December 2007; live attenuated human rotavirus vaccine; GlaxoSmithKline; oral given on 31 July 2007; pneumococcal vaccine, unspecified; manufacturer unspecified; intramuscular; given on 31 July 2007 and 1 October 2007; tuberculosis vaccine; manufacturer unspecified; intradermal; given on 9 February 2008. On 1 October 2007, the subject received 2nd dose of ROTARIX (oral), lot number not provided. On 12 February 2008, 4 months after vaccination with ROTARIX, the subject experienced gastric vomiting followed by biliary vomiting with colic and abdominal pain. She had not flatulence nor fever. On 13 February 2008, the subject was hospitalised for 7 days. Physical examination showed abdominal pain with increased peristalsis, dehydration, irritability, crying at abdominal palpation, non-tender abdomen with respiratory pathology. On 14 February 2008, the subject experienced bloody stools as well as biliary vomiting. The rectal examination revealed an empty ampulla with blood. Abdomen X-ray showed fluid levels and dilated bowel loops with non-specific abnormalities. No intussusception was found. The surgery was performed and intussusception of ascending and descending colon was found and resolved by taxis without complication. A prophylactic appendectomy was performed. On 19 February 2008, the events were resolved and the subject was discharged from hospital in good clinical condition. The physician considered the events were unrelated to vaccination with ROTARIX.


Changed on 9/14/2018

VAERS ID: 311332 Before After
VAERS Form:1
Age:0.6
Gender:Female
Location:Foreign
Vaccinated:2007-10-01
Onset:2008-02-12
Submitted:2008-04-30
Entered:2008-04-30
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HEP: HEP B (NO BRAND NAME) / UNKNOWN MANUFACTURER - / 2 UN / IM
PPV: PNEUMO (NO BRAND NAME) / UNKNOWN MANUFACTURER - / 2 UN / IM
RV1: ROTAVIRUS (ROTARIX) / GLAXOSMITHKLINE BIOLOGICALS - / 2 MO / PO

Administered by: Other      Purchased by: Other
Symptoms: Abdominal pain, Appendicectomy, Crying, Dehydration, Haematochezia, Inappropriate schedule of drug administration, Intussusception, Irritability, Surgery, Vomiting, Gastrointestinal hypermotility, Abdominal X-ray

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit (V2.0)? No
ER or Office Visit (V1.0)? No
ER or ED Visit (V2.0)? No
Hospitalized? Yes, days: 7     Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness: Unknown
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Abdominal X-ray 14Feb2008 Abnormal unit
CDC 'Split Type': B0517193A

Write-up: This case was reported by a physician and described the occurrence of intussusception in a 11-month-old female subject who was vaccinated with ROTARIX (GlaxoSmithKline). Previous and/or concurrent vaccination included combined diphtheria, tetanus, acellular pertussis, inactivated poliomyelitis and Haemophilus influenzae type b vaccine; manufacturer unspecified; intramuscular; given on 31 July 2007, 4 December 2007 and an unspecified date; hepatitis B vaccine recombinant; manufacturer unspecified; intramuscular; given on 31 July 2007, 1 October 2007 and 4 December 2007; influenza virus vaccine; manufacturer unspecified; intramuscular; given on 4 December 2007; live attenuated human rotavirus vaccine; GlaxoSmithKline; oral given on 31 July 2007; pneumococcal vaccine, unspecified; manufacturer unspecified; intramuscular; given on 31 July 2007 and 1 October 2007; tuberculosis vaccine; manufacturer unspecified; intradermal; given on 9 February 2008. On 1 October 2007, the subject received 2nd dose of ROTARIX (oral), lot number not provided. On 12 February 2008, 4 months after vaccination with ROTARIX, the subject experienced gastric vomiting followed by biliary vomiting with colic and abdominal pain. She had not flatulence nor fever. On 13 February 2008, the subject was hospitalised for 7 days. Physical examination showed abdominal pain with increased peristalsis, dehydration, irritability, crying at abdominal palpation, non-tender abdomen with respiratory pathology. On 14 February 2008, the subject experienced bloody stools as well as biliary vomiting. The rectal examination revealed an empty ampulla with blood. Abdomen X-ray showed fluid levels and dilated bowel loops with non-specific abnormalities. No intussusception was found. The surgery was performed and intussusception of ascending and descending colon was found and resolved by taxis without complication. A prophylactic appendectomy was performed. On 19 February 2008, the events were resolved and the subject was discharged from hospital in good clinical condition. The physician considered the events were unrelated to vaccination with ROTARIX.

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